Canonical Allele Identifier: CA1565634278

Gene: ERAP2 ERAP1

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.96908845C>G , CM000667.2:g.96908845C>G	GRCh38
NC_000005.9:g.96244549C>G , CM000667.1:g.96244549C>G	GRCh37
NC_000005.8:g.96270305C>G	NCBI36
NG_027839.2:g.32139G>C
NG_051092.1:g.37907C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000510373.6:c.2013-116C>G (ERAP2)	ENSP00000421175.2:n.2013-116C>G
ENST00000437043.8:c.2013-116C>G (ERAP2) MANE Select	ENSP00000400376.3:n.2013-116C>G
ENST00000379904.8:c.1878-116C>G (ERAP2)	ENSP00000369235.4:n.1878-116C>G
ENST00000437043.7:c.2013-116C>G (ERAP2)	ENSP00000400376.3:n.2013-116C>G
ENST00000510373.5:c.2013-116C>G (ERAP2)	ENSP00000421175.1:n.2013-116C>G
ENST00000513084.5:c.*470-116C>G (ERAP2)	ENSP00000421849.1:n.*470-116C>G
ENST00000515387.1:n.744-121C>G (ERAP2)
NM_001130140.1:c.2013-116C>G (ERAP2)	NP_001123612.1:n.2013-116C>G
NM_022350.3:c.2013-116C>G (ERAP2)	NP_071745.1:n.2013-116C>G
XM_011543480.1:c.-706+25277G>C (ERAP1)	XP_011541782.1:n.-706+25277G>C
XM_011543481.1:c.-703+25277G>C (ERAP1)	XP_011541783.1:n.-703+25277G>C
XM_011543482.1:c.-710+25277G>C (ERAP1)	XP_011541784.1:n.-710+25277G>C
XM_011543483.1:c.-873+25277G>C (ERAP1)	XP_011541785.1:n.-873+25277G>C
XM_011543484.1:c.-702+25277G>C (ERAP1)	XP_011541786.1:n.-702+25277G>C
XM_011543485.1:c.-522+25277G>C (ERAP1)	XP_011541787.1:n.-522+25277G>C
XM_011543486.1:c.-706+25277G>C (ERAP1)	XP_011541788.1:n.-706+25277G>C
XM_011543487.1:c.-706+25277G>C (ERAP1)	XP_011541789.1:n.-706+25277G>C
XM_011543544.1:c.1944-116C>G (ERAP2)	XP_011541846.1:n.1944-116C>G
NM_001130140.2:c.2013-116C>G (ERAP2)	NP_001123612.1:n.2013-116C>G
NM_001329229.1:c.1878-116C>G (ERAP2)	NP_001316158.1:n.1878-116C>G
NM_022350.4:c.2013-116C>G (ERAP2)	NP_071745.1:n.2013-116C>G
NR_137637.1:n.2780-116C>G (ERAP2)
XM_011543480.2:c.-706+25277G>C (ERAP1)	XP_011541782.1:n.-706+25277G>C
XM_011543481.2:c.-703+25277G>C (ERAP1)	XP_011541783.1:n.-703+25277G>C
XM_011543484.2:c.-702+25277G>C (ERAP1)	XP_011541786.1:n.-702+25277G>C
XM_011543485.2:c.-522+25277G>C (ERAP1)	XP_011541787.1:n.-522+25277G>C
XM_011543486.3:c.-706+25277G>C (ERAP1)	XP_011541788.1:n.-706+25277G>C
XM_011543544.2:c.1944-116C>G (ERAP2)	XP_011541846.1:n.1944-116C>G
XM_017009581.1:c.-548+25277G>C (ERAP1)	XP_016865070.1:n.-548+25277G>C
XM_024446113.1:c.-545+25277G>C (ERAP1)	XP_024301881.1:n.-545+25277G>C
XR_001742179.2:n.2181-116C>G (ERAP2)
NM_022350.5:c.2013-116C>G (ERAP2) MANE Select	NP_071745.1:n.2013-116C>G